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FDA 510(k)

PDT-FACE

K-Number: K192295 · 2020-05-01

ApplicantBeijing Adss Development Co., Ltd.
Decision Date2020-05-01
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PDT-FACE is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Adss Development Co., Ltd.. It received FDA 510(k) clearance on 2020-05-01 under 510(k) number K192295. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PDT-FACE?

PDT-FACE is a medical device that received FDA 510(k) clearance on 2020-05-01. The listed applicant is Beijing Adss Development Co., Ltd.. The 510(k) number is K192295.

When did PDT-FACE receive FDA 510(k) clearance?

PDT-FACE received FDA 510(k) clearance on 2020-05-01, under 510(k) number K192295.

Who is the listed applicant for PDT-FACE?

The FDA 510(k) record lists Beijing Adss Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PDT-FACE?

The FDA product code for PDT-FACE is OLP.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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